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On the whereabouts of SARS-CoV-2 in the human body: A systematic review

Trypsteen, Wim, Van Cleemput, Jolien, Snippenberg, Willem van, Gerlo, Sarah, Vandekerckhove, Linos·2020·PLOS Pathogens

Abstract

Since SARS-CoV-2 appeared in the human population, the scientific community has scrambled to gather as much information as possible to find good strategies for the containment and treatment of this pandemic virus. Here, we performed a systematic review of the current (pre)published SARS-CoV-2 literature with a focus on the evidence concerning SARS-CoV-2 distribution in human tissues and viral shedding in body fluids. In addition, this evidence is aligned with published ACE2 entry-receptor (single cell) expression data across the human body to construct a viral distribution and ACE2 receptor body map. We highlight the broad organotropism of SARS-CoV-2, as many studies identified viral components (RNA, proteins) in multiple organs, including the pharynx, trachea, lungs, blood, heart, vessels, intestines, brain, male genitals and kidneys. This also implicates the presence of viral components in various body fluids such as mucus, saliva, urine, cerebrospinal fluid, semen and breast milk. The main SARS-CoV-2 entry receptor, ACE2, is expressed at different levels in multiple tissues throughout the human body, but its expression levels do not always correspond with SARS-CoV-2 detection, indicating that there is a complex interplay between virus and host. Together, these data shed new light on the current view of SARS-CoV-2 pathogenesis and lay the foundation for better diagnosis and treatment of COVID-19 patients.

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  • Many human cell types expressing ACE2 in multiple organs can be infected by SARS-CoV-2, including (but not limited to) the lungs, heart, small intestine, and liver.

    “Many human cell types expressing ACE2 in multiple organs can be infected by SARS-CoV-2, including (but not limited to) the lungs, heart, small intestine, and liver45,46.”

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Research works printed but not linked: 194

  1. M Bolles, 2011, SARS-CoV and emergent coronaviruses: viral determinants of interspecies transmission., Current Opinion in Virology, 1, 624, 10.1016/j.coviro.2011.10.012 · DOI
  2. KG Andersen, 2020, The proximal origin of SARS-CoV-2, Nature Medicine, 26, 450, 10.1038/s41591-020-0820-9 · DOI · Paper page
  3. M Hoffmann, 2020, SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor, Cell, 181, 271, 10.1016/j.cell.2020.02.052 · DOI · Paper page
  4. L Lin, 2020, Hypothesis for potential pathogenesis of SARS-CoV-2 infection–a review of immune changes in patients with viral pneumonia., Emerging Microbes & Infections., 9, 727, 10.1080/22221751.2020.1746199 · DOI
  5. JM Connors, 2020, COVID-19 and its implications for thrombosis and anticoagulation, Blood, 135, 2033, 10.1182/blood.2020006000 · DOI
  6. MG Argenziano, 2020, Characterization and clinical course of 1000 patients with coronavirus disease 2019 in New York: retrospective case series., Bmj-British Medical Journal., 369
  7. C Huang, 2020, Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China., Lancet, 395, 497, 10.1016/S0140-6736(20)30183-5 · DOI · Paper page
  8. L Lin, 2020, Gastrointestinal symptoms of 95 cases with SARS-CoV-2 infection, Gut, 69, 997, 10.1136/gutjnl-2020-321013 · DOI
  9. KH Chu, 2005, Acute renal impairment in coronavirus-associated severe acute respiratory syndrome, Kidney Int, 67, 698, 10.1111/j.1523-1755.2005.67130.x · DOI
  10. L Mao, Neurologic Manifestations of Hospitalized Patients With Coronavirus Disease 2019 in Wuhan, China., JAMA neurology, 2020, e201127
  11. X Zou, 2020, Single-cell RNA-seq data analysis on the receptor ACE2 expression reveals the potential risk of different human organs vulnerable to 2019-nCoV infection., Front Med., 14, 185, 10.1007/s11684-020-0754-0 · DOI · Paper page
  12. N Zhu, 2020, A Novel Coronavirus from Patients with Pneumonia in China, 2019., N Engl J Med, 382, 727, 10.1056/NEJMoa2001017 · DOI · Paper page
  13. L Carsana, 2020, Pulmonary post-mortem findings in a series of COVID-19 cases from northern Italy: a two-centre descriptive study, The Lancet Infectious Diseases
  14. V Polat, 2020, Sudden death due to acute pulmonary embolism in a young woman with COVID-19., J Thromb Thrombolysis., 50, 239, 10.1007/s11239-020-02132-5 · DOI
  15. BT Bradley, 2020, Histopathology and Ultrastructural Findings of Fatal COVID-19 Infections., medRxiv., 2020
  16. JX Chaofu Wang, 2020, Aveolar Macrophage Activation and Cytokine Storm in the Pathogenesis of Severe COVID-19 (preprint)., Research Square.
  17. YJ Hou, 2020, SARS-CoV-2 Reverse Genetics Reveals a Variable Infection Gradient in the Respiratory Tract, Cell
  18. P Bost, 2020, Host-Viral Infection Maps Reveal Signatures of Severe COVID-19, Patients. Cell
  19. RL Chua, 2020, Cross-talk between the airway epithelium and activated immune cells defines severity in COVID-19., medRxiv, 2020
  20. NG Ravindra, 2020, Single-cell longitudinal analysis of SARS-CoV-2 infection in human bronchial epithelial cells., bioRxiv, 2020
  21. AJ Venkatakrishnan, 2020, Knowledge synthesis from 100 million biomedical documents augments the deep expression profiling of coronavirus receptors., bioRxiv, 2020
  22. N Saheb Sharif-Askari, 2020, Airways Expression of SARS-CoV-2 Receptor, ACE2, and TMPRSS2 Is Lower in Children Than Adults and Increases with Smoking and COPD., Molecular Therapy—Methods & Clinical Development., 18, 1, 10.1016/j.omtm.2020.05.013 · DOI
  23. L Zou, 2020, SARS-CoV-2 Viral Load in Upper Respiratory Specimens of Infected Patients, N Engl J Med, 382, 1177, 10.1056/NEJMc2001737 · DOI
  24. J Li, 2020, Case Report: Viral Shedding for 60 Days in a Woman with COVID-19, Am J Trop Med Hyg, 102, 1210, 10.4269/ajtmh.20-0275 · DOI
  25. Y-M Qu, 2020, Positive result of Sars-Cov-2 in sputum from a cured patient with COVID-19, Travel Med Infect Dis, 34, 101619, 10.1016/j.tmaid.2020.101619 · DOI
  26. J Huang, 2020, Long period dynamics of viral load and antibodies for SARS-CoV-2 infection: an observational cohort study., medRxiv, 2020
  27. WR Hartman, 2020, Prolonged viral RNA shedding after COVID-19 symptom resolution in older convalescent plasma donors., medRxiv, 2020
  28. XJ Li, 2020, A case of a readmitted patient who recovered from COVID-19 in Chengdu, China., Crit Care., 24, 152, 10.1186/s13054-020-02877-8 · DOI
  29. M Helleberg, 2020, Persistent COVID-19 in an Immunocompromised Patient Temporarily Responsive to Two Courses of Remdesivir Therapy, The Journal of Infectious Diseases
  30. J Bullard, 2020, Predicting infectious SARS-CoV-2 from diagnostic samples, Clinical infectious diseases: an official publication of the Infectious Diseases Society of America, ciaa638, 10.1093/cid/ciaa638 · DOI · Paper page
  31. C-G Huang, 2020, Culture-Based Virus Isolation To Evaluate Potential Infectivity of Clinical Specimens Tested for COVID-19, Journal of Clinical Microbiology, 58, e01068
  32. MM Arons, 2020, Presymptomatic SARS-CoV-2 Infections and Transmission in a Skilled Nursing Facility., New England Journal of Medicine, 382, 2081, 10.1056/NEJMoa2008457 · DOI
  33. B La Scola, 2020, Viral RNA load as determined by cell culture as a management tool for discharge of SARS-CoV-2 patients from infectious disease wards, European Journal of Clinical Microbiology & Infectious Diseases, 39, 1059, 10.1007/s10096-020-03913-9 · DOI
  34. SA Kujawski, 2020, Clinical and virologic characteristics of the first 12 patients with coronavirus disease 2019 (COVID-19] in the United States., Nature Medicine, 26, 861, 10.1038/s41591-020-0877-5 · DOI
  35. H Yao, 2020, Patient-derived mutations impact pathogenicity of SARS-CoV-2., medRxiv, 2020
  36. M Remmelink, 2020, Unspecific post-mortem findings despite multiorgan 1 viral spread in COVID-19 patients., medRxiv, 2020
  37. G Tavazzi, 2020, Myocardial localization of coronavirus in COVID-19 cardiogenic shock, Eur J Heart Fail, 22, 911, 10.1002/ejhf.1828 · DOI
  38. Z Varga, 2020, Endothelial cell infection and endotheliitis in COVID-19, Lancet, 395, 1417, 10.1016/S0140-6736(20)30937-5 · DOI · Paper page
  39. V Monteil, 2020, Inhibition of SARS-CoV-2 Infections in Engineered Human Tissues Using Clinical-Grade Soluble Human ACE2, Cell, 181, 905, 10.1016/j.cell.2020.04.004 · DOI · Paper page
  40. X Xu, 2020, Single-cell Transcriptome Analysis Indicates New Potential Regulation Mechanism of ACE2 and NPs signaling among heart failure patients infected with SARS-CoV-2., medRxiv, 2020
  41. J Guo, 2020, Single-cell RNA Analysis on ACE2 Expression Provides Insight into SARS-CoV-2 Blood Entry and Heart Injury., medRxiv, 2020
  42. Z Ghazizadeh, 2020, Androgen Regulates SARS-CoV-2 Receptor Levels and Is Associated with Severe COVID-19 Symptoms in Men., bioRxiv, 2020
  43. F Hikmet, 2020, The protein expression profile of ACE2 in human tissues., bioRxiv, 2020
  44. S Johri, 2020, Integrated analysis of bulk multi omic and single-cell sequencing data confirms the molecular origin of hemodynamic changes in Covid-19 infection explaining coagulopathy and higher geriatric mortality., medRxiv, 2020
  45. A Moustafa, 2020, Traces of SARS-CoV-2 RNA in the Blood of COVID-19 Patients., medRxiv, 2020
  46. A Banerjee, 2020, Isolation, sequence, infectivity and replication kinetics of SARS-CoV-2., bioRxiv, 2020
  47. CA Hogan, 2020, High frequency of SARS-CoV-2 RNAemia and association with severe disease., medRxiv, 2020
  48. W Chen, 2020, Detectable 2019-nCoV viral RNA in blood is a strong indicator for the further clinical severity., Emerg Microbes Infect, 9, 469, 10.1080/22221751.2020.1732837 · DOI
  49. PHG Duijf, 2020, Baseline pulmonary levels of CD8+ T cells and NK cells inversely correlate with expression of the SARS-CoV-2 entry receptor ACE2., bioRxiv, 2020
  50. U Radzikowska, 2020, Distribution of ACE2, CD147, cyclophilins, CD26 and other SARS-CoV-2 associated molecules in human tissues and immune cells in health and disease., bioRxiv, 2020
  51. S Gupta, 2020, Persistent viral shedding of SARS-CoV-2 in faeces—a rapid review., medRxiv, 2020
  52. S Parasa, 2020, Prevalence of Gastrointestinal Symptoms and Fecal Viral Shedding in Patients With Coronavirus Disease 2019: A Systematic Review and Meta-analysis., JAMA Netw Open, 3, e2011335, 10.1001/jamanetworkopen.2020.11335 · DOI
  53. C Han, 2020, Digestive Symptoms in COVID-19 Patients With Mild Disease Severity: Clinical Presentation, Stool Viral RNA Testing, and Outcomes, Am J Gastroenterol, 115, 916, 10.14309/ajg.0000000000000664 · DOI · Paper page
  54. J Cai, 2020, A Case Series of children with 2019 novel coronavirus infection: clinical and epidemiological features., Clin Infect Dis
  55. JF Chan, 2020, A familial cluster of pneumonia associated with the 2019 novel coronavirus indicating person-to-person transmission: a study of a family cluster., Lancet, 395, 514, 10.1016/S0140-6736(20)30154-9 · DOI
  56. L Chen, 2020, COVID-19 Disease With Positive Fecal and Negative Pharyngeal and Sputum Viral Tests, Am J Gastroenterol, 115, 790, 10.14309/ajg.0000000000000610 · DOI
  57. ML Holshue, 2020, First Case of 2019 Novel Coronavirus in the United States., N Engl J Med, 382, 929, 10.1056/NEJMoa2001191 · DOI · Paper page
  58. T Hosoda, 2020, SARS-CoV-2 enterocolitis with persisting to excrete the virus for approximately two weeks after recovering from diarrhea: A case report, Infect Control Hosp Epidemiol, 41, 753, 10.1017/ice.2020.87 · DOI
  59. JY Kim, 2020, Viral Load Kinetics of SARS-CoV-2 Infection in First Two Patients in Korea, J Korean Med Sci, 35, e86, 10.3346/jkms.2020.35.e86 · DOI
  60. FX Lescure, 2020, Clinical and virological data of the first cases of COVID-19 in Europe: a case series, Lancet Infect Dis, 20, 697, 10.1016/S1473-3099(20)30200-0 · DOI
  61. Y Ling, 2020, Persistence and clearance of viral RNA in 2019 novel coronavirus disease rehabilitation patients., Chin Med J (Engl)., 133, 1039, 10.1097/CM9.0000000000000774 · DOI
  62. IL Lo, 2020, Evaluation of SARS-CoV-2 RNA shedding in clinical specimens and clinical characteristics of 10 patients with COVID-19 in Macau, Int J Biol Sci, 16, 1698, 10.7150/ijbs.45357 · DOI
  63. E Nicastri, 2020, Coronavirus disease (COVID-19] in a paucisymptomatic patient: epidemiological and clinical challenge in settings with limited community transmission, Italy, February 2020., Euro Surveill., 25, 10.2807/1560-7917.ES.2020.25.11.2000230 · DOI
  64. Y Pan, 2020, Viral load of SARS-CoV-2 in clinical samples, Lancet Infect Dis, 20, 411, 10.1016/S1473-3099(20)30113-4 · DOI · Paper page
  65. L Peng, 2020, 2019 Novel Coronavirus can be detected in urine, blood, anal swabs and oropharyngeal swabs samples., medRxiv, 2020
  66. L Song, 2020, A case of SARS-CoV-2 carrier for 32 days with several times false negative nucleic acid tests., medRxiv, 2020
  67. LV Tan, 2020, Duration of viral detection in throat and rectum of a patient with COVID-19., medRxiv, 2020
  68. A Tang, 2020, Detection of Novel Coronavirus by RT-PCR in Stool Specimen from Asymptomatic Child, China, Emerg Infect Dis, 26, 1337, 10.3201/eid2606.200301 · DOI · Paper page
  69. S Wang, 2020, Clinical characteristics and fecal-oral transmission potential of patients with COVID-19., medRxiv, 2020
  70. W Wang, 2020, Detection of SARS-CoV-2 in Different Types of Clinical Specimens, JAMA, 323, 1843
  71. Y Wu, 2020, Prolonged presence of SARS-CoV-2 viral RNA in faecal samples, Lancet Gastroenterol Hepatol, 5, 434, 10.1016/S2468-1253(20)30083-2 · DOI
  72. F Xiao, 2020, Evidence for Gastrointestinal Infection of SARS-CoV-2, Gastroenterology, 158, 1831, 10.1053/j.gastro.2020.02.055 · DOI · Paper page
  73. Y Xing, 2020, Prolonged presence of SARS-CoV-2 in feces of pediatric patients during the convalescent phase., medRxiv, 2020
  74. M Xu, 2020, A Research on the Results of Viral Nucleic Acid Tests and CT Imaging Variation of Patients with COVID-19., medRxiv, 2020
  75. Y Xu, 2020, Characteristics of pediatric SARS-CoV-2 infection and potential evidence for persistent fecal viral shedding, Nat Med, 26, 502, 10.1038/s41591-020-0817-4 · DOI · Paper page
  76. J Zhang, 2020, Fecal specimen diagnosis 2019 novel coronavirus-infected pneumonia., Journal of Medical Virology, 92, 680, 10.1002/jmv.25742 · DOI
  77. N Zhang, 2020, Virus shedding patterns in nasopharyngeal and fecal specimens of COVID-19 patients., medRxiv, 2020
  78. T Zhang, 2020, Detectable SARS-CoV-2 viral RNA in feces of three children during recovery period of COVID-19 pneumonia, Journal of Medical Virology
  79. W Zhang, 2020, Molecular and serological investigation of 2019-nCoV infected patients: implication of multiple shedding routes., Emerg Microbes Infect, 9, 386, 10.1080/22221751.2020.1729071 · DOI
  80. W Tan, 2020, Viral Kinetics and Antibody Responses in Patients with COVID-19., medRxiv, 2020
  81. C Xie, 2020, Comparison of different samples for 2019 novel coronavirus detection by nucleic acid amplification tests., Int J Infect Dis, 93, 264, 10.1016/j.ijid.2020.02.050 · DOI
  82. S Zheng, 2020, Viral load dynamics and disease severity in patients infected with SARS-CoV-2 in Zhejiang province, China, January-March 2020: retrospective cohort study, Bmj, 369, m1443, 10.1136/bmj.m1443 · DOI
  83. 2020, Clinical and virologic characteristics of the first 12 patients with coronavirus disease 2019 (COVID-19] in the United States, Nature Medicine
  84. Z Peng, 2020, Unlikely SARS-CoV-2 vertical transmission from mother to child: A case report, J Infect Public Health, 13, 818, 10.1016/j.jiph.2020.04.004 · DOI
  85. KK-W To, 2020, Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study, Lancet Infectious Diseases, 20, 565, 10.1016/S1473-3099(20)30196-1 · DOI
  86. Y Liu, 2020, Stability of SARS-CoV-2 on environmental surfaces and in human excreta., medRxiv, 2020
  87. L Azzi, 2020, Two cases of COVID-19 with positive salivary and negative pharyngeal or respiratory swabs at hospital discharge: A rising concern, Oral diseases
  88. L Azzi, 2020, Saliva is a reliable tool to detect SARS-CoV-2, The Journal of infection, 81, e45, 10.1016/j.jinf.2020.04.005 · DOI
  89. Chen LaZ, Jiajia and Peng, Jinfeng and Li, Xiaoshuang and Deng, Xuliang and Geng, Zhi and Shen, Zhenyu and Guo, Fengyuan and Zhang, Qianwen and Jin, Yang and Wang, Lin and Wang, Songlin,. Detection of 2019-nCoV in Saliva and Characterization of Oral Symptoms in COVID-19 Patients. SSRN. 2020. · DOI
  90. MS Han, 2020, Sequential analysis of viral load in a neonate and her mother infected with SARS-CoV-2, Clinical infectious diseases: an official publication of the Infectious Diseases Society of America
  91. S Iwasaki, 2020, Comparison of SARS-CoV-2 detection in nasopharyngeal swab and saliva., medRxiv, 2020
  92. AJ Jamal, 2020, Sensitivity of nasopharyngeal swabs and saliva for the detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2]., medRxiv, 2020
  93. Y Tajima, 2020, A case report of SARS-CoV-2 confirmed in saliva specimens up to 37 days after onset: Proposal of saliva specimens for COVID-19 diagnosis and virus monitoring, Journal of infection and chemotherapy: official journal of the Japan Society of Chemotherapy
  94. KK To, 2020, Consistent detection of 2019 novel coronavirus in saliva., Clinical infectious diseases: an official publication of the Infectious Diseases Society of America
  95. KK To, 2020, Temporal profiles of viral load in posterior oropharyngeal saliva samples and serum antibody responses during infection by SARS-CoV-2: an observational cohort study, The Lancet Infectious diseases, 20, 565, 10.1016/S1473-3099(20)30196-1 · DOI
  96. E Williams, 2020, Saliva as a non-invasive specimen for detection of SARS-CoV-2, Journal of clinical microbiology
  97. AL Wyllie, 2020, Saliva is more sensitive for SARS-CoV-2 detection in COVID-19 patients than nasopharyngeal swabs., medRxiv, 2020
  98. JG Yoon, 2020, Clinical Significance of a High SARS-CoV-2, Viral Load in the Saliva. Journal of Korean Medical Science, 35
  99. J Zhu, 2020, Viral dynamics of SARS-CoV-2 in saliva from infected patients, The Journal of infection
  100. VCC Cheng, 2020, Escalating infection control response to the rapidly evolving epidemiology of the coronavirus disease 2019 (COVID-19] due to SARS-CoV-2 in Hong Kong., Infection control and hospital epidemiology., 41, 493, 10.1017/ice.2020.58 · DOI
  101. P Anfinrud, 2020, Could SARS-CoV-2 be transmitted via speech droplets?, medRxiv, 2020
  102. SJ Smither, 2020, Experimental aerosol survival of SARS-CoV-2 in artificial saliva and tissue culture media at medium and high humidity., Emerging microbes & infections., 9, 1415, 10.1080/22221751.2020.1777906 · DOI · Paper page
  103. J Song, 2020, Systematic analysis of ACE2 and TMPRSS2 expression in salivary glands reveals underlying transmission mechanism caused by SARS-CoV-2, Journal of medical virology
  104. J Wang, 2020, ACE2 expression by colonic epithelial cells is associated with viral infection, immunity and energy metabolism., medRxiv, 2020
  105. P Dawson, 2020, Loss of Taste and Smell as Distinguishing Symptoms of COVID-19., medRxiv, 2020
  106. LA Vaira, 2020, Objective evaluation of anosmia and ageusia in COVID-19 patients: Single-center experience on 72 cases, Head and Neck-Journal for the Sciences and Specialties of the Head and Neck
  107. MM Lamers, 2020, SARS-CoV-2 Productively Infects Human Gut Enterocytes., bioRxiv, 2020
  108. Q Wang, 2020, Pattern of liver injury in adult patients with COVID-19: a retrospective analysis of 105 patients., Mil Med Res., 7, 28
  109. Z Fan, 2020, Clinical Features of COVID-19-Related Liver Functional Abnormality, Clin Gastroenterol Hepatol, 18, 1561, 10.1016/j.cgh.2020.04.002 · DOI
  110. A Hadi, 2020, Coronavirus Disease-19 (COVID-19] associated with severe acute pancreatitis: Case report on three family members., Pancreatology., 20, 665, 10.1016/j.pan.2020.04.021 · DOI
  111. F Liu, 2020, ACE2 Expression in Pancreas May Cause Pancreatic Damage After SARS-CoV-2 Infection., Clinical gastroenterology and hepatology: the official clinical practice journal of the American Gastroenterological Association.
  112. X Chai, 2020, Specific ACE2 Expression in Cholangiocytes May Cause Liver Damage After 2019-nCoV Infection., bioRxiv, 2020
  113. JJ Wen Seow, 2020, scRNA-seq reveals ACE2 and TMPRSS2 expression in TROP2+ Liver Progenitor Cells: Implications in COVID-19 associated Liver Dysfunction., bioRxiv
  114. H zhou, 2020, Urinalysis, but not blood biochemistry, detects the early renal-impairment in patients with COVID-19., medRxiv, 2020
  115. G Pei, 2020, Renal Involvement and Early Prognosis in Patients with COVID-19 Pneumonia, J Am Soc Nephrol, 31, 1157, 10.1681/ASN.2020030276 · DOI
  116. B Diao, 2020, Human Kidney is a Target for Novel Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2] Infection., medRxiv, 2020
  117. H Su, Renal histopathological analysis of 26 postmortem findings of patients with COVID-19 in China., Kidney International
  118. M Pesaresi, 2020, SARS-CoV-2 identification in lungs, heart and kidney specimens by transmission and scanning electron microscopy, European Review for Medical and Pharmacological Sciences, 24, 5186
  119. C Fan, 2020, ACE2 Expression in Kidney and Testis May Cause Kidney and Testis Damage After 2019-nCoV Infection., medRxiv, 2020
  120. W Lin, 2020, Single-cell Analysis of ACE2 Expression in Human Kidneys and Bladders Reveals a Potential Route of 2019-nCoV Infection., bioRxiv, 2020
  121. F Hikmet, 2020, The protein expression profile of ACE2 in human tissues., bioRxiv, 2020
  122. X Ren, 2020, Multiple expression assessments of ACE2 and TMPRSS2 SARS-CoV-2 entry molecules in the urinary tract and their associations with clinical manifestations of COVID-19., bioRxiv, 2020
  123. H Stower, 2020, Virological assessment of SARS-CoV-2, Nature medicine, 26, 465
  124. JF Chan, 2020, Improved Molecular Diagnosis of COVID-19 by the Novel, Highly Sensitive and Specific COVID-19-RdRp/Hel Real-Time Reverse Transcription-PCR Assay Validated In Vitro and with Clinical Specimens, J Clin Microbiol, 58
  125. L Wang, 2020, Coronavirus Disease 19 Infection Does Not Result in Acute Kidney Injury: An Analysis of 116 Hospitalized Patients from Wuhan, China., Am J Nephrol., 51, 343, 10.1159/000507471 · DOI
  126. J Sun, 2020, Isolation of infectious SARS-CoV-2 from urine of a COVID-19 patient, Emerg Microbes Infect, 9, 991, 10.1080/22221751.2020.1760144 · DOI
  127. F Pan, 2020, No evidence of severe acute respiratory syndrome–coronavirus 2 in semen of males recovering from coronavirus disease 2019., Fertility and Sterility, 113, 1135, 10.1016/j.fertnstert.2020.04.024 · DOI
  128. C Song, 2020, Absence of 2019 Novel Coronavirus in Semen and Testes of COVID-19 Patients., Biol Reprod
  129. X Liu, 2020, Single-cell transcriptome analysis of the novel coronavirus (SARS-CoV-2] associated gene ACE2 expression in normal and non-obstructive azoospermia (NOA) human male testes., Science China-Life Sciences
  130. Z Wang, 2020, scRNA-seq Profiling of Human Testes Reveals the Presence of the ACE2 Receptor, A Target for SARS-CoV-2 Infection in Spermatogonia, Leydig and Sertoli Cells., Cells, 9, 10.3390/cells9040920 · DOI
  131. A Shastri, 2020, Delayed clearance of SARS-CoV2 in male compared to female patients: High ACE2 expression in testes suggests possible existence of gender-specific viral reservoirs., medRxiv, 2020
  132. D Li, 2020, Clinical Characteristics and Results of Semen Tests Among Men With Coronavirus Disease 2019., JAMA network open., 3, e208292, 10.1001/jamanetworkopen.2020.8292 · DOI
  133. D Paoli, 2020, Study of SARS-CoV-2 in semen and urine samples of a volunteer with positive naso-pharyngeal swab, Journal of Endocrinological Investigation
  134. w quan, 2020, No SARS-CoV-2 in expressed prostatic secretion of patients with coronavirus disease 2019: a descriptive multicentre study in China., medRxiv, 2020
  135. P Cui, 2020, Clinical features and sexual transmission potential of SARS-CoV-2 infected female patients: a descriptive study in Wuhan, China., medRxiv, 2020
  136. RN Baergen, 2020, Placental Pathology in Covid-19 Positive Mothers: Preliminary Findings., Pediatr Dev Pathol., 23, 177, 10.1177/1093526620925569 · DOI
  137. Y Chen, 2020, Infants Born to Mothers With a New Coronavirus (COVID-19], Frontiers in Pediatrics, 8, 10.3389/fped.2020.00104 · DOI
  138. R Pique-Regi, 2020, Does the human placenta express the canonical cell entry mediators for SARS-CoV-2?, bioRxiv, 2020
  139. H Chen, 2020, Clinical characteristics and intrauterine vertical transmission potential of COVID-19 infection in nine pregnant women: a retrospective review of medical records, The Lancet, 395, 809, 10.1016/S0140-6736(20)30360-3 · DOI
  140. E Kalafat, 2020, Lung ultrasound and computed tomographic findings in pregnant woman with COVID-19., Ultrasound in Obstetrics & Gynecology., 55, 835, 10.1002/uog.22034 · DOI
  141. Y Li, 2020, Lack of Vertical Transmission of Severe Acute Respiratory Syndrome Coronavirus 2, China, Emerging infectious diseases, 26, 1335, 10.3201/eid2606.200287 · DOI
  142. J Goad, 2020, Female reproductive tract has low concentration of SARS-CoV2 receptors., bioRxiv, 2020
  143. MS Han, 2020, Sequential analysis of viral load in a neonate and her mother infected with SARS-CoV-2, Clin Infect Dis
  144. A Coronado Munoz, 2020, Late-Onset Neonatal Sepsis in a Patient with Covid-19, N Engl J Med, 382, e49, 10.1056/NEJMc2010614 · DOI
  145. N Nathan, 2020, Atypical presentation of COVID-19 in young infants, Lancet, 395, 1481, 10.1016/S0140-6736(20)30980-6 · DOI
  146. M Knight, 2020, Characteristics and outcomes of pregnant women admitted to hospital with confirmed SARS-CoV-2 infection in UK: national population based cohort study, Bmj, 369, m2107, 10.1136/bmj.m2107 · DOI
  147. C Rodrigues, 2020, Pregnancy and breastfeeding during COVID-19 pandemic: A systematic review of published pregnancy cases., medRxiv, 2020
  148. R Groß, 2020, Detection of SARS-CoV-2 in human breastmilk., The Lancet, 395, 1757, 10.1016/S0140-6736(20)31181-8 · DOI
  149. Wu Yanting LC, Dong Lan, Zhang Chenjie, Chen Yang, Liu Jun, Zhang Chen, Duan Chenchi, Zhang Hanqiu, Mol Ben Willem, Dennis Cindy-Lee, Yin Tailang, Yang Jing, Huang He-Feng. Viral Shedding of COVID-19 in Pregnant Women. 2020. · DOI
  150. CD Chambers, 2020, Evaluation of SARS-CoV-2 in Breastmilk from 18 Infected Women., medRxiv, 2020
  151. R Bernard-Valnet, 2020, Two patients with acute meningo-encephalitis concomitant to SARS-CoV-2 infection., medRxiv, 2020
  152. P Alberti, 2020, Guillain-Barré syndrome related to COVID-19 infection., Neurol Neuroimmunol Neuroinflamm., 7, 10.1212/NXI.0000000000000741 · DOI
  153. A Benussi, 2020, Clinical characteristics and outcomes of inpatients with neurological disease and COVID-19., medRxiv, 2020
  154. R Yin, 2020, Clinical characteristics of 106 patients with neurological diseases and co-morbid coronavirus disease 2019: a retrospective study., medRxiv, 2020
  155. DC Hess, 2020, COVID-19-Related Stroke., Translational Stroke Research
  156. N Poyiadji, 2020, COVID-19-associated Acute Hemorrhagic Necrotizing Encephalopathy: CT and MRI Features., Radiology., 201187
  157. L Zanin, 2020, SARS-CoV-2 can induce brain and spine demyelinating lesions, Acta Neurochirurgica
  158. T Zhang, 2020, COVID-19-Associated Acute Disseminated Encephalomyelitis: A Case Report., medRxiv, 2020
  159. L Zhou, Sars-Cov-2: Underestimated damage to nervous system., Travel Med Infect Dis, 2020, 101642
  160. A Filatov, 2020, Neurological Complications of Coronavirus Disease (COVID-19]: Encephalopathy., Cureus, 12, e7352
  161. G Novi, 2020, Acute disseminated encephalomyelitis after SARS-CoV-2 infection., Neurol Neuroimmunol Neuroinflamm., 7, 10.1212/NXI.0000000000000797 · DOI
  162. T Schaller, 2020, Postmortem Examination of Patients With COVID-19, JAMA
  163. R Chen, 2020, The spatial and cell-type distribution of SARS-CoV-2 receptor ACE2 in human and mouse brain., bioRxiv, 2020
  164. S Shiers, 2020, ACE2 expression in human dorsal root ganglion sensory neurons: implications for SARS-CoV-2 virus-induced neurological effects., bioRxiv, 2020
  165. L Fodoulian, 2020, SARS-CoV-2 receptor and entry genes are expressed by sustentacular cells in the human olfactory neuroepithelium., bioRxiv, 2020
  166. B Bozkurt, 2020, The COVID-19 Pandemic: Clinical Information for Ophthalmologists., Turk J Ophthalmol., 50, 59, 10.4274/tjo.galenos.2020.29805 · DOI
  167. L Chen, 2020, Ocular manifestations and clinical characteristics of 534 cases of COVID-19 in China: A cross-sectional study., medRxiv, 2020
  168. J Xia, 2020, Evaluation of coronavirus in tears and conjunctival secretions of patients with SARS-CoV-2 infection., Journal of medical virology
  169. H-T Xie, 2020, SARS-CoV-2 in the ocular surface of COVID-19 patients., Eye and Vision., 7
  170. K Kumar, 2020, Presence of viral RNA of SARS-CoV-2 in conjunctival swab specimens of COVID-19 patients., Indian J Ophthalmol., 68, 1015, 10.4103/ijo.IJO_1287_20 · DOI
  171. P Wu, 2020, Characteristics of Ocular Findings of Patients With Coronavirus Disease 2019 (COVID-19] in Hubei Province, China., Jama Ophthalmology, 138, 575, 10.1001/jamaophthalmol.2020.1291 · DOI
  172. Y Zhou, 2020, Ophthalmologic evidence against the interpersonal transmission of 2019 novel coronavirus through conjunctiva., medRxiv, 2020
  173. L Chen, 2020, Ocular manifestations of a hospitalised patient with confirmed 2019 novel coronavirus disease., British Journal of Ophthalmology, 104, 748, 10.1136/bjophthalmol-2020-316304 · DOI
  174. IYJ Seah, 2020, Assessing Viral Shedding and Infectivity of Tears in Coronavirus Disease 2019 (COVID-19] Patients., Ophthalmology
  175. l Xu, 2020, Conjunctival polymerase chain reaction-tests of 2019 novel coronavirus in patients in Shenyang,China., medRxiv, 2020
  176. K Hamashima, 2020, Potential modes of COVID-19 transmission from human eye revealed by single-cell atlas., bioRxiv, 2020
  177. L Zhou, 2020, ACE2 and TMPRSS2 are expressed on the human ocular surface, suggesting susceptibility to SARS-CoV-2 infection., bioRxiv, 2020
  178. R Gianotti, 2020, Cutaneous Clinico-Pathological Findings in three COVID-19-Positive Patients Observed in the Metropolitan Area of Milan, Italy., Acta Derm Venereol., 100, adv00124, 10.2340/00015555-3490 · DOI
  179. B Joob, 2020, COVID-19 can present with a rash and be mistaken for dengue, J Am Acad Dermatol, 82, e177, 10.1016/j.jaad.2020.03.036 · DOI
  180. S Recalcati, 2020, Cutaneous manifestations in COVID-19: a first perspective, Journal of the European Academy of Dermatology and Venereology, 34, e212, 10.1111/jdv.16387 · DOI
  181. P van der Voort, 2020, A clinical and biological framework on the role of visceral fat tissue and leptin in SARS-CoV-2 infection related respiratory failure., medRxiv, 2020
  182. SA Heialy, 2020, Regulation of angiotensin converting enzyme 2 (ACE2] in obesity: implications for COVID-19., bioRxiv, 2020
  183. K Nakagawa, 2016, Viral and Cellular mRNA Translation in Coronavirus-Infected Cells., Adv Virus Res, 96, 165, 10.1016/bs.aivir.2016.08.001 · DOI
  184. JV Forrester, 2018, Ebola virus and persistent chronic infection: when does replication cease?, Ann Transl Med., 6, S39, 10.21037/atm.2018.09.60 · DOI
  185. JC Smith, 2020, Cigarette Smoke Exposure and Inflammatory Signaling Increase the Expression of the SARS-CoV-2 Receptor ACE2 in the Respiratory Tract, Developmental Cell, 53, 514, 10.1016/j.devcel.2020.05.012 · DOI
  186. S Rao, 2020, Exploring Diseases/Traits and Blood Proteins Causally Related to Expression of ACE2, the Putative Receptor of SARS-CoV-2: A Mendelian Randomization Analysis Highlights Tentative Relevance of Diabetes-Related Traits, Diabetes Care, dc200643
  187. M Jacobs, 2020, Increased expression of ACE2, the SARS-CoV-2 entry receptor, in alveolar and bronchial epithelium of smokers and COPD subjects., medRxiv, 2020
  188. B Bénéteau-Burnat, 1990, Serum angiotensin-converting enzyme in healthy and sarcoidotic children: comparison with the reference interval for adults, Clin Chem, 36, 344, 10.1093/clinchem/36.2.344 · DOI
  189. J Chen, 2020, Individual variation of the SARS-CoV-2 receptor ACE2 gene expression and regulation, Aging Cell, 19, e13168, 10.1111/acel.13168 · DOI · Paper page
  190. E Ciaglia, 2020, COVID-19 Infection and Circulating ACE2 Levels: Protective Role in Women and Children., Frontiers in Pediatrics, 8
  191. T Jefferson, Viral cultures for COVID-19 infectivity assessment. Systematic review., medRxiv, 2020, 2020
  192. CS Goldsmith, 2020, Electron microscopy of SARS-CoV-2: a challenging task, Lancet, 395, e99, 10.1016/S0140-6736(20)31188-0 · DOI
  193. SS Lakdawala, 2020, The search for a COVID-19 animal model., Science, 368, 942, 10.1126/science.abc6141 · DOI
  194. SN Ehaideb, 2020, A systematic review uncovers a wide-gap between COVID-19 in humans and animal models., medRxiv, 2020

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Metadata

Authors
Trypsteen, W., Van Cleemput, J., Snippenberg, W. V., Gerlo, S., & Vandekerckhove, L.
Venue
PLOS Pathogens
Published
2020-10-30
Volume
16
Issue
10
Pages
e1009037
ISSN
1553-7374
Cited by
199
References
14
Language
en

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